1. 'Fly-ing' from rare to common neurodegenerative disease mechanisms. Issue 9 (September 2022) Authors: Ma, Mengqi; Moulton, Matthew J.; Lu, Shenzhao; Bellen, Hugo J. Journal: Trends in genetics Issue: Volume 38:Issue 9(2022) Page Start: 972 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms. Issue 16 (26th March 2022) Authors: Huang, Yan; Ma, Mengqi; Mao, Xiao; Pehlivan, Davut; Kanca, Oguz; Un-Candan, Feride; Shu, Li; Akay, Gulsen; Mitani, Tadahiro; Lu, Shenzhao; Candan, Sukru; Wang, Hua; Xiao, Bo; Lupski, James R; Bellen, Hugo J Journal: Human molecular genetics Issue: Volume 31:Issue 16(2022) Page Start: 2751 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival. Issue 6 (18th October 2022) Authors: Ma, Mengqi; Zhang, Xi; Zheng, Yiming; Lu, Shenzhao; Pan, Xueyang; Mao, Xiao; Pan, Hongling; Chung, Hyung-lok; Wang, Hua; Guo, Hong; Bellen, Hugo J Journal: Human molecular genetics Issue: Volume 32:Issue 6(2023) Page Start: 984 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗